Cargando…

A genetic screen in Arabidopsis reveals the identical roles for RBP45d and PRP39a in 5’ cryptic splice site selection

Cryptic splice sites in eukaryotic genome are generally dormant unless activated by mutation of authentic splice sites or related splicing factors. How cryptic splice sites are used remains unclear in plants. Here, we identified two cryptic splicing regulators, RBP45d and PRP39a that are homologs of...

Descripción completa

Detalles Bibliográficos
Autores principales: Huang, Weihua, Zhang, Liqun, Zhu, Yajuan, Chen, Jingli, Zhu, Yawen, Lin, Fengru, Chen, Xiaomei, Huang, Jirong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9813592/
https://www.ncbi.nlm.nih.gov/pubmed/36618610
http://dx.doi.org/10.3389/fpls.2022.1086506
_version_ 1784863953966333952
author Huang, Weihua
Zhang, Liqun
Zhu, Yajuan
Chen, Jingli
Zhu, Yawen
Lin, Fengru
Chen, Xiaomei
Huang, Jirong
author_facet Huang, Weihua
Zhang, Liqun
Zhu, Yajuan
Chen, Jingli
Zhu, Yawen
Lin, Fengru
Chen, Xiaomei
Huang, Jirong
author_sort Huang, Weihua
collection PubMed
description Cryptic splice sites in eukaryotic genome are generally dormant unless activated by mutation of authentic splice sites or related splicing factors. How cryptic splice sites are used remains unclear in plants. Here, we identified two cryptic splicing regulators, RBP45d and PRP39a that are homologs of yeast U1 auxiliary protein Nam8 and Prp39, respectively, via genetic screening for suppressors of the virescent sot5 mutant, which results from a point mutation at the 5’ splice site (5’ ss) of SOT5 intron 7. Loss-of-function mutations in RBP45d and PRP39a significantly increase the level of a cryptically spliced variant that encodes a mutated but functional sot5 protein, rescuing sot5 to the WT phenotype. We furtherly demonstrated that RBP45d and PRP39a interact with each other and also with the U1C, a core subunit of U1 snRNP. We found that RBP45d directly binds to the uridine (U)-rich RNA sequence downstream the 5’ ss of SOT5 intron 7. However, other RBP45/47 members do not function redundantly with RBP45d, at least in regulation of cryptic splicing. Taken together, RBP45d promotes U1 snRNP to recognize the specific 5’ ss via binding to intronic U-rich elements in plants.
format Online
Article
Text
id pubmed-9813592
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-98135922023-01-06 A genetic screen in Arabidopsis reveals the identical roles for RBP45d and PRP39a in 5’ cryptic splice site selection Huang, Weihua Zhang, Liqun Zhu, Yajuan Chen, Jingli Zhu, Yawen Lin, Fengru Chen, Xiaomei Huang, Jirong Front Plant Sci Plant Science Cryptic splice sites in eukaryotic genome are generally dormant unless activated by mutation of authentic splice sites or related splicing factors. How cryptic splice sites are used remains unclear in plants. Here, we identified two cryptic splicing regulators, RBP45d and PRP39a that are homologs of yeast U1 auxiliary protein Nam8 and Prp39, respectively, via genetic screening for suppressors of the virescent sot5 mutant, which results from a point mutation at the 5’ splice site (5’ ss) of SOT5 intron 7. Loss-of-function mutations in RBP45d and PRP39a significantly increase the level of a cryptically spliced variant that encodes a mutated but functional sot5 protein, rescuing sot5 to the WT phenotype. We furtherly demonstrated that RBP45d and PRP39a interact with each other and also with the U1C, a core subunit of U1 snRNP. We found that RBP45d directly binds to the uridine (U)-rich RNA sequence downstream the 5’ ss of SOT5 intron 7. However, other RBP45/47 members do not function redundantly with RBP45d, at least in regulation of cryptic splicing. Taken together, RBP45d promotes U1 snRNP to recognize the specific 5’ ss via binding to intronic U-rich elements in plants. Frontiers Media S.A. 2022-12-22 /pmc/articles/PMC9813592/ /pubmed/36618610 http://dx.doi.org/10.3389/fpls.2022.1086506 Text en Copyright © 2022 Huang, Zhang, Zhu, Chen, Zhu, Lin, Chen and Huang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Huang, Weihua
Zhang, Liqun
Zhu, Yajuan
Chen, Jingli
Zhu, Yawen
Lin, Fengru
Chen, Xiaomei
Huang, Jirong
A genetic screen in Arabidopsis reveals the identical roles for RBP45d and PRP39a in 5’ cryptic splice site selection
title A genetic screen in Arabidopsis reveals the identical roles for RBP45d and PRP39a in 5’ cryptic splice site selection
title_full A genetic screen in Arabidopsis reveals the identical roles for RBP45d and PRP39a in 5’ cryptic splice site selection
title_fullStr A genetic screen in Arabidopsis reveals the identical roles for RBP45d and PRP39a in 5’ cryptic splice site selection
title_full_unstemmed A genetic screen in Arabidopsis reveals the identical roles for RBP45d and PRP39a in 5’ cryptic splice site selection
title_short A genetic screen in Arabidopsis reveals the identical roles for RBP45d and PRP39a in 5’ cryptic splice site selection
title_sort genetic screen in arabidopsis reveals the identical roles for rbp45d and prp39a in 5’ cryptic splice site selection
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9813592/
https://www.ncbi.nlm.nih.gov/pubmed/36618610
http://dx.doi.org/10.3389/fpls.2022.1086506
work_keys_str_mv AT huangweihua ageneticscreeninarabidopsisrevealstheidenticalrolesforrbp45dandprp39ain5crypticsplicesiteselection
AT zhangliqun ageneticscreeninarabidopsisrevealstheidenticalrolesforrbp45dandprp39ain5crypticsplicesiteselection
AT zhuyajuan ageneticscreeninarabidopsisrevealstheidenticalrolesforrbp45dandprp39ain5crypticsplicesiteselection
AT chenjingli ageneticscreeninarabidopsisrevealstheidenticalrolesforrbp45dandprp39ain5crypticsplicesiteselection
AT zhuyawen ageneticscreeninarabidopsisrevealstheidenticalrolesforrbp45dandprp39ain5crypticsplicesiteselection
AT linfengru ageneticscreeninarabidopsisrevealstheidenticalrolesforrbp45dandprp39ain5crypticsplicesiteselection
AT chenxiaomei ageneticscreeninarabidopsisrevealstheidenticalrolesforrbp45dandprp39ain5crypticsplicesiteselection
AT huangjirong ageneticscreeninarabidopsisrevealstheidenticalrolesforrbp45dandprp39ain5crypticsplicesiteselection
AT huangweihua geneticscreeninarabidopsisrevealstheidenticalrolesforrbp45dandprp39ain5crypticsplicesiteselection
AT zhangliqun geneticscreeninarabidopsisrevealstheidenticalrolesforrbp45dandprp39ain5crypticsplicesiteselection
AT zhuyajuan geneticscreeninarabidopsisrevealstheidenticalrolesforrbp45dandprp39ain5crypticsplicesiteselection
AT chenjingli geneticscreeninarabidopsisrevealstheidenticalrolesforrbp45dandprp39ain5crypticsplicesiteselection
AT zhuyawen geneticscreeninarabidopsisrevealstheidenticalrolesforrbp45dandprp39ain5crypticsplicesiteselection
AT linfengru geneticscreeninarabidopsisrevealstheidenticalrolesforrbp45dandprp39ain5crypticsplicesiteselection
AT chenxiaomei geneticscreeninarabidopsisrevealstheidenticalrolesforrbp45dandprp39ain5crypticsplicesiteselection
AT huangjirong geneticscreeninarabidopsisrevealstheidenticalrolesforrbp45dandprp39ain5crypticsplicesiteselection